Aurobindo Pharma Hiring Regulatory Affairs (CMC) Roles

Regulatory Affairs Job for M.Pharm Graduates (2-5 Yrs) | Aurobindo Pharma Hyderabad

 Apply for Regulatory Affairs (CMC) job at Aurobindo Pharma, Hyderabad. M.Pharm with 2-5 yrs experience in Topical & Derma US Regulatory Affairs required.

Join Aurobindo Pharma: Regulatory Affairs (CMC) Role for Experienced M.Pharm Professionals in Hyderabad

Are you an M.Pharm graduate with a strong background in US regulatory affairs? Aurobindo Pharma, a global leader in generics and specialty formulations, is hiring skilled professionals for the Regulatory Affairs (CMC) department, focusing on Topical & Derma products for the US market.

This opportunity is ideal for candidates with 2 to 5 years of experience who want to work in a dynamic and innovation-driven pharmaceutical environment in Hyderabad, Telangana.

Why Choose Aurobindo Pharma?

Aurobindo Pharma is committed to a healthier life through excellence in research, development, and regulatory operations. With global outreach and strong regulatory compliance standards, it’s the right platform to grow your pharma career.

About the Job Role

Designation: Regulatory Affairs (CMC) – Topical & Derma – US Market

Location: APLRC1, Hyderabad, Telangana – 500090

Experience Required: 2–5 Years in Regulatory Affairs (US Market)

Job Type: Full-Time, On-Site

Key Responsibilities

• Review of manufacturing and analytical documents including specifications, test procedures, and validation reports
• Review and preparation of regulatory dossiers for Topical and Derma products in the US market
• Compile and submit eCTD modules (Module 2 & 3)
• Perform CMC documentation tasks for solid and liquid oral dosage forms
• Ensure compliance with ICH guidelines and regulatory standards
• Participate in extractable & leachable studies, stability protocols, and dissolution protocol reviews

Essential Skills and Competencies

• Strong knowledge of eCTD software and electronic submissions
• Familiarity with Topical and Derma product regulatory requirements (mandatory)
• Working experience in reviewing CMC documents
• Proficiency in MS Office, documentation, and regulatory research
• Basic understanding of ICH guidelines and global regulatory standards

Required Educational Qualification

• M.Pharm (Master of Pharmacy) in Pharmaceutics or related specialization

How to Apply?

Interested and qualified candidates can send their updated resume to:

📩 Email: Hrrc1@aurobindo.com

Take the next step in your career by joining a reputed global pharmaceutical company with a strong regulatory portfolio.

Eligibility-Based Courses (For Keyword Optimization)

• M.Pharm (Pharmaceutics, Regulatory Affairs, Industrial Pharmacy)
• Pharmaceutical Technology, Drug Regulatory Affairs, Quality Assurance

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